Now look at Omicron spike protein 671-692.
Two amino acid changes and one is the infamous proline change near the FCS. Prolines are right angle brackets in proteins. When they change, they alter structure.
P681H
N679K
This may attenuate the SEB toxicity. Fewer Ckine storms.
Ahanotu et al considerations on SEB as a bioweapon as prescient.
Some of this is discussed in our preprint.
I was not aware of these SEB mutations in omicron when I wrote this.
I was C19 +ve when I submitted this, ironically.
Of note, They find a pango-lineage (B.1.596 - not to be confused with Omicron B.1.1.529) that has these mutations that would make for higher homology to the toxins.
This lineage broke out in the US and Kenya. It didn't get very far. cov-lineages.org/lineage.html?l…
You can see its prevalence in blue. Delta replaced it.
Wonder if these were sicker cases? Anyone have IFR by Pango-lineage? Is there even any signal with all the confounders?
We keep debating the IFR of the most prevalent strains but should we? outbreak.info/location-repor…
The most prevalent strains are unlikely to be the most lethal. Note the Proline mutation in question is flagged (yellow) as Variants Of Interest (VOI) (P681H). As is N679K. Both are are not observed in the other lineages on display.
Cheng et al followed up with a paper in Cell showcasing an antibody that blocked SEB/FCS.
Look at how sensitive the FCS codons are. By using the rarest codon in human cells, stack two rare events next to each other and you get ribosomal pausing which in turn is required for spike to fold properly.
It is well known from BioNtech (Lenk et al) and Sutton et al (1997) that RNA:DNA hybrids inhibit DNaseI.
What is less known is that Quadruplex Gs also inhibit DNaseI. Some exist in SV40 and we get the most signal from this qPCR amplicon.
2 Different mechanisms of DNaseI inhibition = plasmid fragmentation cannot be assumed to be uniform in the mRNA vaccines. Hence 100 fold more spike than parts of the vector.
Below is a map of the codon optimized spike where Quadruplex Gs are overlaid with GAA repeats. GAA's are stickier RNA:DNA hybrids.
Our qPCR primers are overlayed as well.
@RetsefL @KUPERWASSERLAB @weldeiry @JesslovesMJK @DJSpeicher @TracyBethHoeg @DrJBhattacharya
Evans et al demonstrate DNaseI is resistant to quadruplex Gs. They also move to alternative enzymes. nature.com/articles/s4152…
This is from Lenk et al (BioNtech).
Note the concern over GAA sequences and RNA:DNA hybrids.
Our spike qPCR primers happen to land on GAA rich and quadruplex G rich regions of Spike. frontiersin.org/journals/molec…
@LocasaleLab I find the RNAi worship incongruent will how that entire field was ignored when injecting billions of people with mRNAs.
There are multiple 21bp homologies to human that emerged from the haphazard codon optimizations in the modRNA vaccine and no one cared?
@LocasaleLab Receipts.
Take Pfizers vax Sequence and run it through BLAT.
Hello... anyone from the RNAi space want to speak up about this?
On Veterans Day @CharlesRixey @JesslovesMJK
Stopped by MGC.
2 long days later we had all of his data.
It’s now published in The Journal of Independent Medicine.
It describes the mechanism of failure for the DNA contamination in the mRNA shots and why the regulators are missing it.
@JesslovesMJK @CharlesRixey @weldeiry @KUPERWASSERLAB @RetsefL @DrJBhattacharya @RWMaloneMD @RobertKennedyJr @TracyBethHoeg
Another Achs et al Fumble uncovered.
These folks don't even understand Capillary Electrophoresis.
Its becoming increasingly clear these are not honest mistakes but designed to deceive by people who are employed at a Vaccine Research Institute.
Science for Sale.
@JesslovesMJK @DJSpeicher
Here is the Rub.
They used a CE instrument that has a lower limit of sensitivity above the 10ng limit.
You need to be able to pick up 10X below the 10ng limit. Or 33pg/ul (300ul dose @ 10ng = 33pg/ul)
This is embarrassingly rigged or they are incompetent.
They ignored our comments on the preprint server and raced their paper into @Nature.
@JesslovesMJK and @DJSpeicher have their own substacks picking up other errors in this paper I'll post sortly.